Lomar srl
IT-MF-000013947 · Italy · Flero (BS)
Lomar srl is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 12 |
|---|---|
| Class IIa | 8 |
Most frequent device types declared: Barra porta accessori, Lomar Medical Testaletto, Lomar Medical Testaletto Gas.
Among these devices, 19 are declared active.
Devices declared under this manufacturer
- Aura compact
- Barra porta accessori
- Combi Gas
- Combi Gas B
- Intensiva P
- Intensiva SDC
- Intensiva SDI
- Intensiva SI
- Start
- Start V
- Start mini
- Style L
Showing 12 of 20 declared devices.
Catalogue references include Aura compact, Barra porta accessori, Combi Gas, Combi Gas B, Intensiva P, Intensiva SDC.
European nomenclature codes declared: Z129017, V0880.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Lomar srl was not found in either the U.S. or the Canadian register.